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China Regulatory Consulting for Medical Device

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Be Aware of CFD...

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China Regulatory Consulting for Medical Device | cirs-md.com Reviews

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China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Be Aware of CFD...

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1 cirs home

2 disclaimer

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5 regulations and know how

6 services

7 clinical trial consulting

8 customs clearance

9 china authorized representative

10 case studies

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China Regulatory Consulting for Medical Device | cirs-md.com Reviews

https://cirs-md.com

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Be Aware of CFD...

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cmdrd.cirs-md.com

China Medical Device Regulatory Database

Medical Devices Classification Search System(MDCSS). Input product identifier and verification code;. View classification and relevant information of your product;. Input your email address. And send the search result with initial regulatory compliance proposals. To your email;. Medical Devices Classification System (MDCS). Device for body fluid transportation. Devices for alteration of blood and body fluids. Devices for medical dressing. Other general passive medical devices. Device for ionized radiation.

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China Authorized Representative - Solutions & Case Studies - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/solutions_and_case_studies/china_authorized_representative

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Having an indep...

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Disclaimer - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/disclaimer

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. And we respect ...

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Regulations & Know-how - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/regulations_and_know_how

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Pre-assessment ...

4

Clinical Trial Consulting - Services - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/services/clinical_trial_consulting

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Class II and cl...

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Pre-market Investigation & Analysis - Services - China Regulatory Consulting for Medical Device

http://www.cirs-md.com/services/pre_market_investigation_and_analysis

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. The first impor...

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cirs-reach.com

News, Events and Newsletters | CIRS

http://www.cirs-reach.com/news.html

You are here: Home. Sign up for Newsletter. Forbidden Declare in Chinese Label for Infant Formula. Imported Dietary Supplements without Blue Hat Registration have been Investigated by Chinese Government. Seminar on the interpretation of the latest regulations concerning hazardous chemicals and introduction to the China GHS. 6 August 2015, Free Webinar: Registration of New and Existing Substance in Taiwan. Free Webinar: Back to Basics - Understanding China's Chemical Regulations. South Korea to Prolong th...

cirs-group.com

Chemical Inspection and Regulation Service(CIRS)

http://www.cirs-group.com/en

Tel : 86 0571-87206555. Fax : 86 0571-87206533. 2016-08-15 - - CIRS Completed the Hundredth Typical Notification under China REACH. 2016-08-15 - - China National Standards (GB) and Regulations Collection and Download. 2016-08-15 - - SMCR 2016 Take Attendees to Experience G20 City Hangzhou. 2016-08-15 - - Asia-Pacific Chemical Inventory Search System Formally Goes Online. 2016-08-15 - - New Labelling Requirements for the Efficacy of Sunblock Available in China.

cirs-reach.com

Chemical Inspection and Regulation Service | Enabling Chemical Compliance for A Safer World | CIRS

http://www.cirs-reach.com/index.html

You are here: Home. Forbidden Declare in Chinese Label for Infant Formula. Imported Dietary Supplements without Blue Hat Registration have been Investigated by Chinese Government. Seminar on the interpretation of the latest regulations concerning hazardous chemicals and introduction to the China GHS. 6 August 2015, Free Webinar: Registration of New and Existing Substance in Taiwan. Free Webinar: Back to Basics - Understanding China's Chemical Regulations. South Korea to Prolong the Term of Regulatory Com...

cirs-group.com

中国医疗器械法规咨询|杭州瑞旭产品技术有限公司|CIRS

http://www.cirs-group.com/md

Howmedica Osteonics Corp.对关节手术工具进行召回. CFDA发布YY 0017 2016 骨接合植入物金属接骨板等64项医疗器械行业标准. 海南省医疗器械经营企业批发零售医疗器械经营质量管理规范现场检. 邮箱 zjj@cirs-group.com. 邮箱 Xuyn@cirs-group.com. 电话 353 41 9806 916. 邮箱 service@cirs-reach.com. 地址杭州市滨江区秋溢路288号东冠高新科技园1号楼11层电话 0571-87206555 传真 0571-87206533.

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杭州瑞旭科技集团有限公司

400电话 : 4006 721 722. 2018-03-20 - 新政解读农药登记资料转让和农药委托加工、分装. 2018-03-20 - 免费网络研讨会 2017年中国化妆品法规更新. 2018-02-12 - 瑞旭技术参加ChemCon The Americas 2018. 2018-02-07 - 瑞旭技术携手韩国咨询公司Chemtopia 成功举办欧洲及亚太地区法规研讨会圆满归来.

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Powered by intrafox Health Care. Über CIRS Health Care. CIRS in der Praxis. Dienstleistung, Schulung and Consulting. Einrichtungsübergreifendes CIRS im Gesundheitsbereich. Fälle - Analysen - Maßnahmen - Hilfsmittel. Über CIRS Health Care. CIRS Health Care ist das webbasierte Fehlermeldesystem für den Austausch von einrichtungsübergreifend interessanten CIRS-Meldungen. Und in der Praxis bereits bewährten Maßnahmen. Für den sofortigen Einsatz im Krankenhaus. Das Patientenrechtegesetz und CIRS. Nicht nur be...

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China Regulatory Consulting for Medical Device

China Regulatory Consulting for Medical Device. Pre-market Investigation and Analysis. Medical Device Registration and Approval. Manufacturing and Distributing License Approval. Quality Assurance and Compliance. Risk Assessment and Management. IPR Protection in China. Solutions and Case Studies. China Medical Device Regulatory Assistant Program (MDRAP). China Medical Device Regulatory Database (CMDRD). Applicable Standards and Technical Requirements. Qualified Testing Institutes in China. Be Aware of CFD...

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